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Publication numberUS3541729 A
Publication typeGrant
Publication dateNov 24, 1970
Filing dateMay 9, 1968
Priority dateMay 9, 1968
Publication numberUS 3541729 A, US 3541729A, US-A-3541729, US3541729 A, US3541729A
InventorsPhilip Dantowitz
Original AssigneeGen Electric
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Compact reactor-boiler combination
US 3541729 A
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Description  (OCR text may contain errors)

P. DANTOWITZ COMRACT REACTOR'BOILER COMBINATION Nov. 24, 1970 2 Sheets-She-et 1 Filed May 9, 1968 INVENTOR IPHILIP DANTOWITZ BY QMMJQML HIS ATTORNEY.

Nov. 24, 1970 COMPACT Filed May 9. 1968 P. DANTowlrz 3,541,729

REACTOR-BOILER COMBINATION 2 Sheets-Sheet 2 F I G 2 I N V E N TO R t PHILIP DANTow T2,

HIS ATTORNEY United States Patent U.S. Cl. 48-94 3 Claims ABSTRACT OF THE DISCLOSURE A fuel for a fuel cell unit is prepared by feeding a mixture of reformable fuel and steam to a catalyst bed in indirect heat transfer relation with a hot iluid stream. The hot filuid is then passed into indirect heat transfer relation with a water reservoir of a surrounding boiler portion. The reaction products including hydrogen received from the catalyst bed are fed into indirect heat transfer relationship with the water reservoir. Steam from the boiler is mixed with the incoming fuel.

BACKGROUND OF THE INVENTION In indirect feed fuel cell systems a hydrocarbon or a partially oxidized derivative, such as an alkanol, aldehyde, ketone, carboxylic acid, etc., may be chemically reacted to liberate free hydrogen before the feed is brought into contact with the anode of a fuel cell. In one conventional approach the fuel is mixed with steam and reformed upstream of the fuel cell anode to liberate free hydrogen. The free hydrogen, usually in a reformate mixture including other reaction products and residual reactants, is fed to a fuel cell anode.

In reacting a reformable fuel and water to produce a hydrogen containing reformate utilizable at a fuel cell anode it is necessary to perform a number of operations. The water must be heated and converted to steam to assure thorough mixing with the reformable fuel. The mixed fuel and steam are brought into contact with a catalyst and react endothermally to produce the hydrogen containing reformate. This means that heat must be continuously supplied in order to drive the reaction. Generally the reaction products leave the catalyst bed at a much higher temperature than can be tolerated by the particular type of fuel cell unit being operated. Accordingly, it is usually desirable that at least some heat be dissipated from the fuel stream prior to reaching the fuel cell unit. Additionally, it is usually also desirable to perform a supplemental reaction to reduce the proportion of carbon monoxide associated with the free hydrogen and thereby minimize anode catalyst poisoning. To avoid poisoning the reforming catalyst, it may also be desirable to preliminarily desulfurize the reformable fuel prior to reforming.

Various systems and methods for reforming a feed stock prior to delivery of a fuel cell anode are disclosed by :Bartas in patent application Ser. No. 530,188, iiled Feb. 25, 1966, titled System and Process for the Indirect Electrochemical Combination of Air and a Reformable Fuel and Chludzinski et al. in patent application Ser. No. 546,326, filed Apr. 29, 1966, and now abandoned titled System and Process Employing a Reformable Fuel to Generate Electrical Energy. 'Ihese disclosures, here incorporated by reference, are typical of prior systems for processing and delivering a fuel cell feed stock in that a m 3,541,729 Patented Nov. 24, 1970 ice I number of separate heat exchange structures are utilized in preparing the fuel for anode consumption. While this approach is advantageous in that simple, conventional exchangers can for the most part be utilized, the use of a number of separate elements in a system results in a system having a. relatively large volume displacement. Where a high degree of compactness and portability are required these systems may not be fully acceptable.

BRIEF SUMMARY OF THE INVENTION It is an object of my invention to provide a compact and efficient unit for contacting lluid reactants with a catalyst bed to produce reaction products.

It is another object of my invention to provide an apparatus capable of eiiiciently converting a mixture of a reformable fuel and steam to a hydrogen containing reformate feed stock suitable for consumption by a fuel cell unit.

These and other objects of my invention are accomplished in one aspect by providing an apparatus comprised of a means providing a source of hot fluid. A reaction sub-assembly is mounted to receive the hot fluid nteriorly thereof and includes a catalyst bed. Means are provided for confining the catalyst bed in indirect heat transfer relation with the hot iluid. Means are provided for directing fluid reactants into contact with the catalyst bed, and means are provided for receiving iiuid reaction products from the catalyst bed. A boiler sub-assembly is mounted exteriorly of the reaction sub-assembly and includes an annular housing means denng a water reservoir. Means are provided for receiving the hot iiuid from the reaction sub-assembly and for directing the hot iiuid into indirect heat transfer relation with the water within the reservoir.

BRIEF DESCRIPTION OF THE DRAWINGS My invention may be better understood by reference to the following detailed description of the invention considered in conjunction with the drawings, in which:

FIG. l is a vertical section with parts broken away and schematically illustrated, and

FIG. 2 is a schematic diagram of a simple system for the utilization of my apparatus.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT In FIG. 1 my inventive reformer unit 1 is shown formed of a hot fluid source 3y which may be merely a conduit for the delivery of a hot fluid, but in most instances is a burner which produces hot iiuid by combusting a fuel and air inside the unit. The unit is also comprised of a reaction sub-assembly 5 and a boiler sub-assembly 7. It is a significant feature of my invention that the reformer unit can be easily disassembled into sub-assemblies, and either the hot iluid source or reaction sub-assembly can be quickly withdrawn from the unit for servicing without disassembling the remaining portions of the reformer unit.

The reaction sub-assembly is comprised of a shell 9 having a cylindrical outer wall 11 connected at its lower end to a cylindrical inner wall 13 by an annular bottom wall 15. The upper end of the cylindrical inner wall is integrally joined to a frusto-conical baille wall 17. Mounted concentrically between the inner and outer cylindrical walls of the shell is a cylindrical partition 19. Located above the partition is a reactant inlet conduit 21. The upper end of the inlet conduit s litted with a threaded plug 23. A side arm is provided to introduce the reactants into the inlet conduit. The reactant inlet conduit is integrally joined to the partition by a swedged transition section 27. The lower end of the partition is spaced from the bottom wall of the shell to provide for Iiluid passage therebetween. A screen 29 is connected between the lower end of the partition and the bottom wall to hold a catalyst bed 31 in position between the partition and inner cylindrical wall of the shell. An annular closure plate 33 sealingly cooperates with the shell and is centrally connected to an outlet conduit 35 having a side arm connection 37. An annular closure plate 39 is provided to close the upper end of the outlet conduit. Overlying the annular closure 33 is a body of thermal insulation 41. Two semi-circular guard plates 43 overlie the thermal insulation.

The boiler sub-assembly is provided with a cylindrical inner wall 45 concentrically spaced from an inner reservoir wall 47. An annular ilange 49 extends inwardly from the inner reservoir wall and is spaced below the lower end of the inner wall. As shown in the drawing the inner reservoir wall is formed integrally at its upper end with an outwardly extending annular wall 51 which in turn is formed integrally with an upwardly extending annular Wall 53. A hot fluid outlet conduit 55 is attached to the upwardly extending annular wall. The inner cylindrical wall is shown formed integrally with an outwardly flared wall 57 which is in turn formed integrally with a support wall 59. The support wall transmits the weight of the inner cylindrical wall to the outwardly extending annular wall. The support wall is apertured at 61 for the passage of hot iluid therethrough. An annular ring 62 iits between the support wall and the upwardly extending wall to assure spacing therebetween and form an annular plenum between the apertures and the hot iluid outlet.

. The inner cylindrical wall is noted to be provided with a mounting flange 63 adjacent its upper end. The mounting ilange supports the reaction sub-assembly, since the shell is provided with a ilange 65 that overlies the mounting flange. A sealing gasket 67 is provided between the mating ilanges, and bolts 69 are provided for a releasable connection between the boiler and reaction sub-assemblies.

An outer reservoir wall 71 is concentrically spaced from the inner reservoir wall, except at its upper and lower extremities, which are sealed to the inner reservoir wall. Thus, an annular reservoir is formed between these two walls. A water inlet conduit 73 is provided adjacent the lower end of the outer reservoir wall while a first steam outlet conduit 75 is provided adjacent the upper end of this wall. For purposes of monitoring the boiler, a water outlet conduit 77 is also provided adjacent the lower end of the outer reservoir wall and connects to a liquid level controller 79, which is schematically illustrated. A second steam outlet conduit 81 also connects to the liquid level controller through a pressure relief valve 83.

A reformate confining wall 85 is spaced concentrically from the outer reservoir wall, but is sealingly attached thereto at its upper and lower extremities. Adjacent its lower end the reformate confining wall is provided with reformate outlet apertures 87. An annular plenum wall 89 cooperates with the confining wall above and below the apertures and carries a reformate outlet conduit 91. Adjacent the upper end of the confining wall reformate inlet apertures 93 are provided which are similarly covered by an upper plenum wall 95 provided with a reformate inlet conduit 97.

A hot fluid source is shown provided with a flange 99 at its upper extremity which seals with annular ilange 49 through an interposed gasket 101. The flanges 49 and 99 are preferably held in assembled relation by bolts, not shown. Beneath the annular flange and exteriorly of the hot iluid source thermal insulation 103 is provided. An annular guard 105 fits over the fluid source to protect and confine the thermal insulation. The annular guard 4 cooperates with the lower extremity of the inner reservoir wall for mounting.

An annular thermally insulative baille 107 is positioned centrally of the reaction sub-assembly. The baille is supported by the annular flange 49. An annular thermally insulative shield 109 is also located between the boiler sub-assembly and the reaction sub-assembly.

From the foregoing description of the structure of the reformer unit 1 it is apparent that the side arm 25, reactant inlet conduit 21, and the spacing between the shell 11 and swedged transition portion 27 and partition 19 together form a reactant inlet passage 111 extending from the exterior of the reformer unit to the upper surface of the catalyst bed. The catalyst vbed is fluid penetrable. Typically the catalyst is present in particulate form. For the purpose of reforming a hydrocarbon fuel or a partially oxidized derivative thereof by interaction with steam the catalyst may, for example, be comprised of particles of nickel supported on alumina, silica, or alumina-silica. Reforming catalysts are per se will known and per se form no part of my invention. It is noted that a wide range of suitable catalysts are reported by Dirksen et al. in Research Bulletin No. 20, titled Improvement of Nickel Cracking Catalysts, published October 1952, by the Institute of Gas Technology, and in Research Bulletin No. 4, titled Effect of Hydrogen Suliide on Catalyst Activity in the Steam Propane Reaction, published at the same time by the same source. The space between the partition and the outer wall 11 of the shell together with the space between the reactant inlet conduit and the reaction product outlet conduit as well as the side arm 37 form a passage 113 whereby reaction products and residual reactants may be removed from the reformer unit.

The insulative baille 107 defines an introductory hot iluid passage segment 115. The annulus between the insulative baille and the inner cylindrical wall 13 of the shell forms a catalyst heating segment 117 of the hot iluid passage. The annulus between the cylindrical inner wall `45 and inner reservoir wall 47 provides an annular boiler heating segment 119 of the hot iluid passage. The hot fluid passage is terminally defined by the hot iluid plenum and the hot iluid outlet conduit 55.

The reformer unit may be constructed by conventional manufacturing techniques. In a preferred form the unit is formed of corrosion resistant metal, such as stainless steel, which is suitably bent and welded to construct the sub-assemblies described above. The reaction sub-assembly is prepared for operation by removing the threaded plug and introducing a particulate reforming catalyst to form the catalyst bed 31. The plug is then sealingly reunited to the inlet conduit 21. The reaction sub-assembly is placed in position on the gasket 67 and mounting flange 63 of the boiler assembly, and the bolts 69 are used to hold the two sub-assemblies firmly united. The thermal insulation 41 is then positioned over the reaction sub-assembly and the semi-circular guard plates 43 fitted over the thermal insulation.

The hot fluid source 3 is positioned with the flange 99 pressed against the flange 49 with gasket 101 interposed. The hot iluid source is illustrated only schematically. This portion of the apparatus may be a burner or merely a iluid conduit. Typically the source is fixedly and releasably attached to the boiler sub-assembly by bolting to the flange 49. After the source is located in position, thermal insulation 103 is fitted around the source and the annular guard 105 is mounted in position. Typically the guard is mechanically and releasably joined to the inner reservoir wall 47.

To place the reformer unit in operation, water, ndicated by flow arrows 121, is introduced into the boiler reservoir 123. The level of the water within the boiler reservoir is continuously controlled by the liquid level controller 79. It is noted that the rst steam outlet conduit 75 communicates with the reactant inlet passage 111 so that immediately upon heating the water within the boiler reservoir steam is produced and fed to the reaction subassembly. The flow path of the steam is schematically illustrated by flow arrows 125.

To generate steam and to bring the catalyst bed to the active reforming temperature hot fluid, indicated schematically by ow arrows 127, is released from the source 3 and passes through the introductory passage segment 115 to the catalyst heating segment 117. In the introductory passage segment of the hot fluid passage loss of heat from the hot iluid is held to a minimum by the thermally insulative baffle 107. Within the catalyst heating passage segment the hot fluid is in indirect heat transfer relation with the catalyst bed. Only the inner cylindrical wall of the shell separates the hot fluid and the catalyst. The insulative baille serves the important function of directing the hot fluid so that it uniformly contacts the inner cylindrical Wall of the shell. This is important, since the chemical reaction taking place within the catalyst bed is endothermic and removes considerable heat from the hot fluid. If the hot fluid transferred heat to one portion of the catalyst bed preferentially, this area could be overheated so as to overheat the catalyst while other portions of the catalyst bed might remain below optimum temperature for eicient performance. The hot fluid passes from indirect heat transfer relation with the catalyst bed to indirect heat transfer relation with the `water within the boiler reservoir. Only the inner reservoir wall 47 separates the hot tluid within the passage segment 119 from the Water within the reservoir. The hot fluid passes from the reformer unit through the outlet conduit 55.

Either simultaneously with the introduction of hot fluid into the reformer unit or at a later time, a reformable fuel, indicated by ilow arrows 129, is introduced into the reactant inlet passage mixed with the steam produced by the boiler subassembly. When the catalyst bed has been heated to operating temperature, the reformable fuel and steam interact upon Contact with the catalyst bed to liberate free hydrogen. Other reaction products formed include carbon dioxide, carbon monoxide, methane, and higher alkanes of lower molecular weight than the reformable fuel. To prevent the formation of carbon within the catalyst bed it is usual practice to operate with an excess of steam so that a substantial portion of steam flows through the catalyst bed unconsumed. Some portion of the reformable fuel also may not be consumed. The aggregate mixture of reaction products and residual unconsumed reactants is termed a reformate. The reformate is schematically indicated by flow arrows 131.

Since the reformate contains a large quantity of heat as it leaves the reaction sub-assembly through the side arm, it is preferred, but not essential, to utilize the reformate as an indirect heat transfer medium. In FIG. 1 this is schematically illustrated by directing the reformate from the reaction sub-assembly to the reformate inlet conduit 97 of the boiler sub-assembly. En route the reformate may be passed through a conventional indirect heat exchanger 133, schematically shown, to transfer heat from the reformate to the reforrnable fuel. In one form it iS anticipated that the reformate may deliver heat to the reformable fuel by indirect heat transfer while the reformable fuel is in contact with a desulfurization catalyst. In this circumstance the reformable fuel can be not only heated but also relieved of any sulfur content that might tend to poison the reforming catalyst bed. Instead of utilizing heat from the reformate, a fraction of the hot iluid may be diverted from the hot fluid passage segment 115 for use in the heat exchanger 133. A preferred arrangement for desulfurization of a reformate is disclosed by Kegan in copending application Ser. No. 727,872, now abandoned, led on even date herewith, the disclosure of which is here incorporated by reference. Where the reformate is to be ultimately supplied to a fuel cell unit it may also be desirable to convert a portion of the carbon monoxide present in the reformate to carbon dioxide. For

this purpose a conventional shift reactor is schematically illustrated positioned downstream of the desulfurizer but upstream of the boiler sub-assembly.

The reformate in being circulated between the outer reservoir wall 71 and the reformate confining wall 85 transfers heat to the water within the boiler reservoir. The reformate upon nally leaving the reformer unit may be reduced in temperature to a level which can be tolerated by a fuel cell unit without appreciable further coollng.

As will readily be apparent the absolute temperature levels of the various portions of my reformer unit may be varied appreciably. The relative temperatures of fiuid in indirect heat transfer relation may be controlled not only by regulating their temperatures, but also by controlling their velocities and volumes. Additionally the thermal characteristics of the separating layer as well as the incorporation or exclusion of heat transfer ns or their equivalent can greatly affect the heat transfer characteristics.

Where a hydrocarbon fuel is being reformed it is preferred that the hot fluid be supplied by burning a portion of the fuel in air Within the reformer unit. This provides a source of hot fluid at temperatures in the range of from 1500 to 2000" F. Since reforming temperatures may range from 750 to l600 F., adequate temperature differential may be obtained to thermally drive the reforming reaction. The velocity of the hot fluid may be sufficiently high to prevent the catalyst bed from heating to llame temperature and being damaged. For example, with nickel catalysts it is usually desirable to maintain the catalyst lbed below 1200 F. during reforming to avoid sintering the catalyst into a composite structure that cannot be conveniently removed from the reaction sub-assembly. By the time the hot uid is lbrought into indirect heat transfer relation with the water within the boiler reservoir a considerable amount of heat has been given up to drive the reforming reaction. Accordingly, the hot fluid is at a considerably reduced temperature, but still well above the 212 F. required to produce steam at atmospheric pressure. By flowing the reformate through the reformer unit countercurrent to the tlow of water to the boiler reservoir, it is apparent that the reformate may actually be cooled to a temperature below the boiling point of water on exhaust. This relationship is of signicance, ysince many aqueous electrolyte fuel cell units operate in temperature range between ambient temperature and the boiling point of water. It is recognized, of course, that many fuel cells, including some aqueous electrolyte fuel cells, operate efficiently at higher ternperatures. Accordingly, cooling the reformate below the boiling temperature of water is by no means essential. It is desirable that the reformate be flowed in a downward direction to allow water condensed by cooling the reformate to be easily removed.

Desulfurization is conveniently effected in the temperature range of from 500 to 600 F. while the conversion of carbon monoxide to carbon dioxide in a reformate stream, conventionally referred to as a shift reaction, can be performed in the temperature range of from 500 to 550 F. These temperatures are noted to be intermediate the temperature of the reformate as it leaves the catalyst bed and the temperature required for steam generation in the boiler sub-assembly. It is anticipated that the reformable fuel may be initially chosen to have such a low sulfur content that desulfurization is unnecessary; hence no desulfurizer may be provided. In this circumstance the reformable fuel may be introduced into the passage 111 in liquid form and vaporized as it travels toward the catalyst bed. Also, where carbon monoxide can be tolerated in the reformate, as in a fuel cell unit which utilizes a palladium foil anode or hydrogen separation barrier, the shift reactor may be eliminated. It is also anticipated that the shift catalyst may, if desired, be located within the reaction sub-assembly within the 7 reaction product passage 113. It is recognized that some adjustment of the location of thermally conductive and thermally insulating members may be required to maintain the shift catalyst at the proper temperature of operation. For example, the partition 19 may be formed of a thermally insulative material.

My apparatus is particularly well suited for processing the fuel feed stock supplied to a fuel cell unit. A Very simple system for the utilization of my apparatus shown in FIG. 1 is schematically diagrammed in FIG. 2. The system 200 is provided with a water source 202 which delivers water to the boiler sub-assembly of the reformer assembly 204 as indicated schematically by pump 206. Flow arrow 121 indicates the flow of water. At the same time a reformable fuel source 208 supplies reformable fuel, indicated by flow arrow 129, to the reformer assembly through pump 210. Hot fluid, indicated by flow arrows 127, passes through the reformer assembly to provide indirect heat exchange and thereby generate reformate, indicated by flow arrow 131. The reformate is fed directly to a fuel cell unit 212. The fuel cell unit, which may be any conventional fuel cell or battery capable of electrochemically oxidizing hydrogen, is also supplied with a conventional oxidant, indicated by flow arrows 214. An electrical load 216 is shown connected to the fuel cell unit by means of electrical leads 218 and 220.

The system 200 is intended merely to illustrate the utility of my invention and is not intended to imply that that the application of my invention is limited thereto, since it is recognized that a number of diverse applications for my invention will be readily apparent to those skilled in the art. For example, while I have disclosed by my invention with reference to the steam reformation of a hydrocarbon or hydrocarbon derivative fuel, it is appreciated that the structural combination designated as a reformer unit may be applied to use with a wide range of chemical reactions. For example, instead of placing a reforming catalyst within the reformer unit as described, a shift catalyst may be placed with the unit instead. It is anticipated that iron oxide, mixtures of zinc and copper oxides, or any other conventional catalyst for shifting the equilibrium in a reformate from carbon monoxide to carbon dioxide may be substituted for the reforming catalyst. The temperature of the incoming hot fluid used for heating may be adjusted to provide the optimum reaction temperature. In such application reformate rather than a reformable fuel and steam mixture would be fed to the reaction sub-assembly. In another variation, a desulfurization catalyst may be utilized in place of a reforming catalyst. In this case the reformable fuel alone without steam mixed is fed to the reaction sub-assembly. The temperature of the hot fluid would again be adjusted to the optimum temperature level of desulfurization. It is recognized that the same catalysts are on occasion used for reforming and shifting as are used for desulfurization, so that it is not essential to even change catalysts in order to achieve this varied application. It is recognized that in its broadest aspects my invention apparatus may be utilized to accomplish any reaction of a fluid in a catalyst bed, since the fluid centrally supplied may be either a hot fluid or a cold fluid and hence suitable either for supplying or removing heat to maintain the desired reaction.

It is recognized that the construction of the reformer unit shown in FIG. l may be varied considerably without departing from my invention. For example, instead of forming the unit by welding together metal sheet stock, the elements of the unit may be formed by any conventional technique and united to form the disclosed structural arrangement. For example, the various elements may be bolted together using gasketing for sealing Where desired. Also, elements of the unit may be integrally cast. It is not necessary that the unit be formed annularly as illustrated. The unit may be provided with a polygonal geometry. It is also anticipated that one or more of the various annuli may be broken up into a plurality of angularly distributed passages. Spacers may be placed within the unit where required to hold the elements concentrally arranged. The reformate confining wall may be omitted where it is not desired to use the reformate to aid in heating the water reservoir. It is not essential that the reformate outlet conduit of the reaction sub-assembly be concentric with the reactant inlet conduit. Also, the reformate may be transmitted from the reaction subassembly lby providing a suitable passage through the unit rather than routing the reformate through external conduits. It is anticipated that the partition may be omitted from at least the lower portion of the shell and the catalyst bed will lie on both sides of the partition or in contact with both the inner and outer walls of the shell. In this circumstance an annular baffle may be provided to bring the hot fluid into intimate contact with both the inner and outer surfaces of the shell. The use of thermal insulation is optional. While thermal insulation is shown adjacent the upper and lower ends of the unit, it may be omitted entirely or additional insulation may be employed to cover the entire external surface as Well as the external fluid conduits (preferred under most ambient conditions), depending upon ambient conditions and the degree of thermal efficiency desired. It is immaterial whether the insulative baflle is formed as part of the source, reaction sub-assembly, or boiler sub-assembly. The reaction subassembly may be supported on the mounting flange as illustrated, or this flange may be omitted and the reaction sub-assembly redesigned to seal against the upper surface of the ring.

Numerous variations will readily occur to those skilled in the art having knowledge of my invention. It is accordingly requested that the scope 0f my invention be determined with reference to the following claims.

Wlhat I claim and desire to secure by Letters Patent of the United States is:

1. An apparatus for reacting a reformable fuel and steam to produce free hydrogen comprising:

means for providing a stream of hot fluid,

a cylindrical reaction sub-assembly mounted to receive the hot fluid interiorly thereof, an annular chamber containing a reforming catalyst spaced from said cylindrical sub-assembly to define a passage for said hot fluid between said annular chamber and said cylindrical sub-assembly,

means for passing said hot fluid in indirect heat transfer relation with said catalyst.

means for directing a mixture of reformable fuel and steam into contact with the reforming catalyst, and means for receiving reaction products including tree hydrogen from said reforming catalyst, and

a boiler sub-assembly mounted exteriorly of said reaction sub-assembly and said annular chamber includmg:

annular (housing means defining a water reservoir spaced from said annular chamber to define a further passage for said hot fluid between said annular chamber and said water reservoir. means for passing the hot fluid from the passage between said cylindrical sub-assembly and said annular chamber and directing the hot fluid into said further passage and thereby into indirect heat transfer relation with the water within the reservoir to convert a portion of the water to steam, and means for directing at least a portion of the steam to said reaction sub-assembly.

2. An apparatus according to claim 1 including means for directing at least a portion of the reaction products to said boiler sub-assembly and said boiler sub-assembly additionally including means for directing the fluid reactants into indirect heat transfer relation with the water within the reservoir.

9 10 3. An apparatus according to claim 2 in which said 3,350,176 10/ 1967 Green et al 48-214 X means for directing reaction products to said boiler sub- 3,438,759 4/ 1969 Linden et al. 48--214 X assembly includes means to react carbon monoxide and 3,469,944 9/ 1969 Bocard et a1. 48-214 X water to produce hydrogen and carbon dioxide.

r MORRIS O. WOLK, Primary Exammer 0 References Cited R. E. SERWIN, Assistant Examiner UNITED STrTES PATENTS US. Cl. X'R- 2,886,507 5/1959 Elliott et al. 48-196 X 23,*212, 288; 48-214; 252-373 3,278,268 10/1966 Pfeferle 48-214 X 10

Patent Citations
Cited PatentFiling datePublication dateApplicantTitle
US2886507 *Jul 7, 1954May 12, 1959Socony Mobil Oil Co IncMethod of supplying endothermic heat of reaction
US3278268 *Aug 15, 1962Oct 11, 1966Engelhard Ind IncMethod for hydrogen production
US3350176 *Mar 24, 1964Oct 31, 1967Engelhard Ind IncHydrogen generator
US3438759 *Dec 3, 1965Apr 15, 1969Cons Natural Gas SvcGas reformer and control means
US3469944 *May 13, 1968Sep 30, 1969Bertrand J MaylandProcess and apparatus for the manufacture of hydrogen for fuel cells
Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US3909299 *Oct 1, 1973Sep 30, 1975United Technologies CorpFuel cell system including reform reactor
US3989480 *Mar 25, 1976Nov 2, 1976The United States Of America As Represented By The United States Energy Research And Development AdministrationDecomposition of carbohydrate wastes
US4026675 *Jun 23, 1975May 31, 1977Friedrich Uhde GmbhHeat exchanger for nuclear reactor installations
US4039584 *Nov 19, 1975Aug 2, 1977Ruhrchemie AktiengesellschaftCatalytic cleavage of isobutyraldehyde
US4071330 *Dec 22, 1976Jan 31, 1978United Technologies CorporationSteam reforming process and apparatus therefor
US4098587 *Aug 25, 1977Jul 4, 1978United Technologies CorporationCompact multi-tube catalytic reaction apparatus
US4098588 *Aug 25, 1977Jul 4, 1978United Technologies CorporationMulti-tube catalytic reaction apparatus
US4098589 *Aug 25, 1977Jul 4, 1978United Technologies CorporationCatalytic reaction apparatus
US4203731 *Dec 15, 1977May 20, 1980Wayne BaileyRadiant energy gasification apparatus
US4323475 *Jun 13, 1980Apr 6, 1982The British Petroleum Company LimitedProcess for the production of amorphous aluminosilicates and their use as catalysts
US4340501 *Sep 2, 1980Jul 20, 1982Imperial Chemical Industries LimitedFluid flow
US4510071 *Aug 1, 1984Apr 9, 1985The British Petroleum Company P.L.C.Methanol conversion process
US4746329 *Nov 26, 1986May 24, 1988Energy Research CorporationMethanol fuel reformer
US4861347 *Dec 29, 1986Aug 29, 1989International Fuel Cells CorporationCompact chemical reaction vessel
US4861348 *Oct 8, 1987Aug 29, 1989Hitachi, Ltd.Fuel reforming apparatus
US4909808 *Oct 14, 1987Mar 20, 1990The United States Of America As Represented By The Administrator Of The National Aeronautics And Space AdministrationSteam reformer with catalytic combustor
US4935037 *Jul 18, 1989Jun 19, 1990Hitachi, Ltd.Reaction tube having endothermic reaction for catalytically reforming fuel gas with steam into hydrogen-enriched gas; heat exchanging; compacts
US5164163 *Sep 12, 1989Nov 17, 1992Kabushiki Kaisha Kobe Seiko ShoHigh efficiency
US5226928 *Dec 24, 1990Jul 13, 1993The Tokyo Electric Power Company, IncorporatedReforming apparatus for hydrocarbon
US5458857 *Nov 22, 1993Oct 17, 1995Rolls-Royce, PlcEfficient
US5565009 *May 23, 1994Oct 15, 1996The Standard Oil CompanyFuel and combustion air are separately heated by heat inside the furnace above their autoignition temperature before being combined in combustion zone, mixing, autoignition and combustion
US5567398 *Jun 16, 1993Oct 22, 1996The Standard Oil CompanyEndothermic reaction apparatus and method
US5618322 *Feb 14, 1994Apr 8, 1997Yamaha Hatsudoki Kabushiki KaishaHaving spirally configured cavity within housing containing catalyst bed heated higher at the inlet than the outlet; by-product inhibition
US5651800 *Jun 7, 1995Jul 29, 1997Yamaha Hatsudoki Kabushiki KaishaReformer for fuel cell system
US5769909 *May 31, 1996Jun 23, 1998International Fuel Cells Corp.Method and apparatus for desulfurizing fuel gas
US6083425 *Nov 2, 1998Jul 4, 2000Arthur D. Little, Inc.Method for converting hydrocarbon fuel into hydrogen gas and carbon dioxide
US6096106 *Feb 3, 1998Aug 1, 2000The Standard Oil CompanyEndothermic reaction apparatus
US6123913 *Nov 3, 1998Sep 26, 2000Arthur D. Little, Inc.Method for converting hydrocarbon fuel into hydrogen gas and carbon dioxide
US6126908 *Aug 26, 1996Oct 3, 2000Arthur D. Little, Inc.Method and apparatus for converting hydrocarbon fuel into hydrogen gas and carbon dioxide
US6153152 *Feb 17, 1998Nov 28, 2000The Standard Oil CompanyUsed ascatalytic reforming apparatus
US6207122Nov 2, 1998Mar 27, 2001Arthur D. Little, Inc.Method for converting hydrocarbon fuel into hydrogen gas and carbon dioxide
US6245303Jan 14, 1998Jun 12, 2001Arthur D. Little, Inc.Reactor for producing hydrogen from hydrocarbon fuels
US6254839Nov 3, 1998Jul 3, 2001Arthur D. Little, Inc.Apparatus for converting hydrocarbon fuel into hydrogen gas and carbon dioxide
US6468480Nov 2, 1998Oct 22, 2002Lawrence G. ClawsonApparatus for converting hydrocarbon fuel into hydrogen gas and carbon dioxide
US6497856Aug 21, 2000Dec 24, 2002H2Gen Innovations, Inc.Reactor with a unitary shell assembly having an inlet and an outlet; a flow path extending within the shell assembly from the inlet to the outlet, the flow path having a steam reformer section with a first catalyst and a water gas shift reactor
US6623719Apr 5, 2002Sep 23, 2003H2Gen InnovationsSystem for hydrogen generation through steam reforming of hydrocarbons and integrated chemical reactor for hydrogen production from hydrocarbons
US6641625May 2, 2000Nov 4, 2003Nuvera Fuel Cells, Inc.Autothermal reformer having distinct zones for partial oxidation reforming and steam reforming, an integrated shift bed for reducing carbon monoxide in product stream, preferential oxidation reactor, and auxiliary reactor
US6645652Sep 28, 2001Nov 11, 2003Ballard Generation Systems Inc.Oxidizers; water circulation; temperature control
US6783742Jun 1, 2001Aug 31, 2004Nuvera Fuel CellsReactor for producing hydrogen from hydrocarbon fuels
US6986797May 2, 2000Jan 17, 2006Nuvera Fuel Cells Inc.Auxiliary reactor for a hydrocarbon reforming system
US7037472 *Oct 1, 2001May 2, 2006Tokyo Gas Co., Ltd.Hydrogen gas generator contains a plurality of circular cylinders and gas flow path sections, helical dividing fins or rods and a metal packing for steam-reforming in presence of reforming catalyst, efficient heat exchanging; reducing CO concentration with CO selective oxidation catalyst; for fuel cells
US7066973May 2, 2000Jun 27, 2006Nuvera Fuel CellsIntegrated reformer and shift reactor
US7276096Jun 25, 2004Oct 2, 2007Ultracell CorporationFuel processor dewar and methods
US7367996 *Dec 5, 2001May 6, 2008Nuvera Fuel Cells, Inc.Heat transfer optimization in multi shelled reformers
US7462208Jun 25, 2004Dec 9, 2008Ultracell CorporationPlanar micro fuel processor
US7507384Jun 13, 2003Mar 24, 2009Nuvera Fuel Cells, Inc.Preferential oxidation reactor temperature regulation
US7604673Jun 25, 2004Oct 20, 2009Ultracell CorporationPortable fuel cells; forming hydrogen using catalyst; catalytic reforming; using boiler and burners
US7670394Jun 21, 2006Mar 2, 2010Haldor Topsoe A/SCompact reforming reactor to convert methanol to hydrogen where reformed gas enriched by passage through a Pressure Adsorption Swing; uniform heating of catalyst tubes; heat of combustion transferred by convection to self-circulating gas-liquid mixture via the generated flue gas; fuel cell plants
US7749290 *Jan 19, 2007Jul 6, 2010General Electric CompanyMethods and apparatus to facilitate cooling syngas in a gasifier
US7807129Jul 2, 2007Oct 5, 2010Ultracell Corporationproduces hydrogen from a fuel source; processor comprises a reformer and burner; reformer includes a catalyst that facilitates the production of hydrogen from the fuel source; method comprises supplying inlet process gas or liquid to burner after it has been heated in dewar chamber; efficiency
US7807130Jul 30, 2007Oct 5, 2010Ultracell Corporationproduces hydrogen from a fuel source; processor comprises a reformer and burner; reformer includes a catalyst that facilitates the production of hydrogen from the fuel source; method comprises supplying inlet process gas or liquid to burner after it has been heated in dewar chamber; efficiency
US20120114537 *Jul 15, 2011May 10, 2012In-Hyuk SonReformer
DE2616085A1 *Apr 13, 1976Oct 28, 1976Stone & Webster Eng CorpMit waerme arbeitender reformierofen und diesen enthaltendes reformiersystem
EP0199878A2 *Dec 23, 1985Nov 5, 1986Westinghouse Electric CorporationApparatus for hydrocarbon fuel processing
EP0247384A2 *Apr 30, 1987Dec 2, 1987Hitachi, Ltd.Reformer
EP0600621A1 *Nov 9, 1993Jun 8, 1994Rolls-Royce And Associates LimitedA combined reformer and shift reactor
EP2623194A1 *Jan 24, 2013Aug 7, 2013Delphi Technologies, Inc.Heat exchange reformer with thermal expansion management
WO1997045887A1 *May 27, 1997Dec 4, 1997Int Fuel Cells CorpMethod and apparatus for desulfurizing fuel gas
WO2001020702A2 *Sep 7, 2000Mar 22, 2001Ballard Generation Systems IncFuel cell electric power generation system
WO2002000547A1 *Jun 18, 2001Jan 3, 2002Gavin P TowlerApparatus for producing hydrogen
WO2002000548A1 *Jun 18, 2001Jan 3, 2002Harness John RApparatus for producing hydrogen
WO2005004256A2 *Jun 25, 2004Jan 13, 2005Ultracell CorpAnnular fuel processor and methods
WO2006069057A2 *Dec 19, 2005Jun 29, 2006Jennifer E BrantleyFuel processor for use with portable fuel cells
WO2007000244A1 *Jun 13, 2006Jan 4, 2007Haldore Topsoe AsCompact reforming reactor
Classifications
U.S. Classification48/94, 423/651, 252/373, 48/214.00A, 422/211
International ClassificationC01B3/38, H01M8/06
Cooperative ClassificationC01B3/384, Y02E60/50, H01M8/0631
European ClassificationC01B3/38B, H01M8/06B2B2
Legal Events
DateCodeEventDescription
Mar 25, 1985ASAssignment
Owner name: UNITED TECHNOLOGIES CORPORATION UNITED TECHNOLOGI
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNOR:GENERAL ELECTRIC COMPANY A CORP. NEW YORK;REEL/FRAME:004378/0886
Effective date: 19850215